Friday, January 29, 2010

Hypertonic Saline Solution (7%)

I pulled this cool article about Hypertonic Saline (HTS) from Cystic Fibrosis Worldwide. I thought it was an pretty interesting read and I learned some things about 7% that I had never known before. Also, keep in mind that it is an older article so some of this stuff may seem a little dated. Enjoy!!!


About Hypertonic Saline

Hypertonic Saline (HS) is just a strong salt-water solution. The concentration used is typically about 7% salt - that is, about twice as salty as seawater — although sometimes weaker or stronger concentrations are used. Hypertonic saline can be turned into a mist by a simple device called a nebuliser. The mist can then be inhaled into the lungs.

How Does Hypertonic Saline Help in CF?

When Hypertonic Saline is inhaled into the lungs, the body tries to dilute the strong salt concentration. The cells lining the airways are triggered to release water. This restores the layer of moisture lining the airways, which helps the mucus to clear the same way it does in healthy lungs. You could think of it as the lungs “flushing out” the stagnant, infected mucus.


Studies done during the mid 1990s showed that inhaling nebulised Hypertonic Saline temporarily increases the speed at which mucus is cleared from the lungs. Subsequent short-term trials showed that inhaling nebulised Hypertonic Saline on a regular basis (usually twice per day) improves lung function in PWCF.

What was the recent trial about?

Although the short-term trials were favourable, it was not known whether Hypertonic Saline is safe and effective when used for long periods. The National Hypertonic Saline Trial tested 164 stable subjects with CF aged at least 6 years of age. These subjects were randomly allocated to inhale either 4mL of Hypertonic Saline (7% saline) or 4mL of placebo (a very weak salt solution — less than one third as salty as sea water). Both solutions contained an inert substance to disguise the taste, so subjects didn’t know which solution they were inhaling. The subjects inhaled their allocated solution twice daily for 48 weeks. They kept up all their other standard therapies, and received whatever additional treatment they normally would whenever they had a flare-up. Patients were checked regularly for signs of improvement, as well as for any possible adverse effects.

What did the trial show?

The main outcome of the trial was lung function — a breathing test, which measures how well the lungs, can shift air in and out. The subjects who were inhaling the Hypertonic Saline had a modest rise in their lung function at the first measurement point (that is, after 4 weeks). This improvement was maintained until at least the last measurement point (that is, 48 weeks).
A much greater effect was seen on the flare-ups of lung infection. The subjects who were inhaling Hypertonic Saline had far fewer flare-ups. The flare-ups they did have tended to be milder, not lasting as long. Although both groups of subjects used a lot of antibiotics to try to prevent flare-ups, those inhaling Hypertonic Saline needed significantly fewer “extra” antibiotics for flare-ups.

Those subjects who were inhaling Hypertonic Saline also reported improved attendance at school, work or other usual activities. On average, those inhaling the placebo missed 17 more days of school/work than those inhaling Hypertonic Saline. People inhaling Hypertonic Saline also felt like their overall health and quality of life was better.

Were there any adverse effects?

Hypertonic Saline can cause the airways to narrow — just like they can do in asthma. In the National Hypertonic Saline Trial, all subjects took a drug to open their airways, called a bronchodilator, just before each dose. This was very effective in limiting the amount of airway narrowing. For this reason, it is strongly recommended that:

• people with CF take a bronchodilator before each dose of Hypertonic Saline and that
• people with CF are supervised when they inhale their first dose of Hypertonic Saline.

Their lung function should be measured before and after the dose, to check that the bronchodilator is strong enough to prevent significant airway narrowing.

Those subjects inhaling Hypertonic Saline also reported more coughing during and immediately after their inhalations. Thus, coughing should be expected when using Hypertonic Saline. However, the coughing tended to settle within the first few doses, the first few days, or at the most, the first few weeks. The coughing was severe enough to prevent people from using Hypertonic Saline in the longterm in only a very small number of cases. In practice, a lower concentration of saline may be more tolerable for these people.

The lungs were also assessed very closely for signs that the constant inhalation of Hypertonic Saline was causing more inflammation in the lungs. There was no evidence of this at all. Also, the use of Hypertonic Saline did not affect which bacteria were found in the lungs, nor their concentration in the mucus.

http://www.cfww.org/pub/english/cfwnl/7/619/Hypertonic_Saline_Research

Comments (8)

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I use HS and it workd for me. I don't always like the taste but it works. Thanks for the artical!
My son uses HS twice daily but recently the Dr took him off due to spitting up blood b/c it seemed to irritate the airways and throat. He has used it forever but now is down to just once a day and it does help on getting that yucky mucous out!!
My 14 yr old son just stared hs will see how it works.
I love it! But can only get it in the hospital, as my insurance won't cover it for me to use at home.
This is the only thing aside from Tobramycin that my son has taken where I can actually see a difference in his health. I cannot recommend it enough.
Hi,
I found your blog via Cystic fibrosis Fatboy. I have a son who is 13, and has a rare, genetic condition called Ataxia-Telangiectasia. (www.atcp.org) It's a neurodegenerative condition, and the most common explanation of what it's like is having ALS, CF, and AIDS all wrapped up in one precious human boy. Anyway, his immune deficiencies are a lack of IgA, and IgE. He has frequent pneumonias, pulmonary infections and the most thick, tenacious mucous I've ever encountered. We have a Hill-Rom vest, and he's on multiple nebs, including Tobi and now hypersal. His pulmonologist is having us try hypersal because the insurance company won't approve Pulmozyme twice a day, which is what he's prefer. I'm trying to explore this, and learn more about CF at the same time. Any advice about how to make things better (like what is the best, fastest neb machine? the one we have is awful) would be deeply appreciated. Now I'm going to start reading - thanks,
Janet
P.S. I was told when he was diagnosed at about 3 yrs of age that he would be in a wheelchair by the age of 10 (which happened) and he would probably die in his teens. I'm fighting that second prediction with everything I've got!!! Peace.....
2 replies · active 728 weeks ago
Thank you for sharing your son's story with me. Sounds like he has quite the battle. I'm happy to read that he has you for a mom however cause it sounds like you can handle it and are willing to do anything and everything for your son.

I would suggest searching this blog and checking out CysticLife.org to find answers to your various questions. If you don't find what you're looking for, then feel free to reach out to me with questions of your own.

As far as a faster neb machine - I recommend Mobilaire 50 psi compressor from Invacare. I started using it a couple of years ago and it's made a world of difference in my treatment time!

Thank you for reaching out to me and I hope to talk again.
Ronnie
Thanks for the nebulizer tip, and I will definitely be reading everything on your blog!! Bows (I'm Buddhist, so it's a way of conveying respect i.e. I bow in respect to your journey, not "bows" like, put a bow on that present for me, will ya honey?) ) to you for reaching out to help others. Peace!

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